EP0474649A1 - Zusammensetzung zur behandlung von pflanzen und deren anwendung. - Google Patents

Zusammensetzung zur behandlung von pflanzen und deren anwendung.

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Publication number
EP0474649A1
EP0474649A1 EP90906787A EP90906787A EP0474649A1 EP 0474649 A1 EP0474649 A1 EP 0474649A1 EP 90906787 A EP90906787 A EP 90906787A EP 90906787 A EP90906787 A EP 90906787A EP 0474649 A1 EP0474649 A1 EP 0474649A1
Authority
EP
European Patent Office
Prior art keywords
magnesium
plants
acid carbonate
solution
reactor
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP90906787A
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English (en)
French (fr)
Other versions
EP0474649B1 (de
Inventor
Henri-Rene Langelin
Robert Goffin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lhoist Recherche et Developpement SA
Original Assignee
Lhoist Recherche et Developpement SA
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Filing date
Publication date
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Publication of EP0474649A1 publication Critical patent/EP0474649A1/de
Application granted granted Critical
Publication of EP0474649B1 publication Critical patent/EP0474649B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05D—INORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
    • C05D7/00—Fertilisers producing carbon dioxide
    • C—CHEMISTRY; METALLURGY
    • C05—FERTILISERS; MANUFACTURE THEREOF
    • C05D—INORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
    • C05D5/00—Fertilisers containing magnesium

Definitions

  • the present invention relates to a process for the treatment of chlorophyll plants, in particular, the curative treatment of chlorophyll plants suffering from primary magnesium deficiencies and the preventive treatment of deficiencies induced by nutritional imbalances or ecophysiological conditions.
  • a process for the treatment of chlorophyll plants in particular, the curative treatment of chlorophyll plants suffering from primary magnesium deficiencies and the preventive treatment of deficiencies induced by nutritional imbalances or ecophysiological conditions.
  • the metabolic activity of a plant is dependent on a large number of factors, the most important of which are environmental factors, notably the climate and the mineral diet (N, P, K, etc.). cier the effect of a factor on this activity, it is essential on the one hand to control all the other factors by keeping them constant (in particular light, humidity and temperature), and on the other hand, it is necessary have a certain number of appropriate techniques allowing this activity to be appreciated in a rapid and non-destructive manner. Maintaining constant light, temperature and mineral nutrition is impractical in open fields, hence the need to carry out these cultures under controlled conditions, for example in a thermostatically controlled culture chamber where all the factors are main ⁇ held constant.
  • Mg ions are much more mobile in the phloem and can be easily transferred from older leaves to young leaves, the apex or the reserve organs of the plains.
  • magnesium an element very important in the plant: it participates in the phosphorylation process where it forms a bridge between the pyrophosphate form of ATP or ADP and the enzyme molecule, which leads to activation of ATPase.
  • Other enzymes such as dehydrogenation and enolase are also activated by the Mg ion.
  • Another key function of magnesium is the activation of ribulose-diphosphate-carboxylase.
  • the illumination of the leaf leads to a massive entry of the Mg ion into the stroma in exchange for protons (H), which creates the optimum conditions for the activity of the carboxylase. This favorable effect of the Mg ion in the assimilation of CO 2 and the production of sugars which is associated with it is probably the consequence of the activation of ribulose-diphosphate-carboxylase.
  • the cation Mg 2+ is the most important cation in the neutralization of diffusible anions in thylacoid membranes.
  • magné ⁇ sium the proportion of nitrogen in reduced protein form and the non-protein form increases.
  • Protein deficiency is probably caused by the dissociation of ribosomes as subunits in the absence of Mg ion. Magnesium appears to stabilize ribosomes in the configuration necessary for protein synthesis.
  • magnesium deficiency differs according to the plant species, but certain general characteristics are the same.
  • a magnesium deficiency manifests itself first on the old leaves, the symptoms then winning in the young leaves.
  • the blade takes a yellow color until necrosis while the veins remain green.
  • Photosynthesis is the basis of the plant's metabolism through the essential role it plays in the conversion of light energy into chemical energy usable by all metabolic and synthesis processes. It is a complex operation in which there are two kinds of reactions. Some, called clear reactions, because they are directly dependent on light, provide the photochemical act, by which light energy is converted into metabolites, the starting point for carbonaceous synthesis and sources of chemical energy. The very au ⁇ , called dark reactions, surround the act chemical photo ⁇ , providing the starting metabolites and I e extend towards the syntheses or reconstitution of the precursors. The photochemical act is only possible through the intervention of assimilating pigments.
  • PS2 there are two photoreceptor systems, one operating in the red on relatively low wavelengths (around 680 nm) called PS2, the other on higher wavelengths (700 nm) is called PSI. These two photosystems are linked by an electron transfer chain made up of guinones, plastoquinones and cytochromes.
  • the pigments on the leaves of plants absorb light, the energy of which is used in the primary photochemical reactions of photosynthesis. Part of the energy The absorbed light is however dissipated in the form of heat (approximately 80%) or re-emitted in the form of fluorescence (approximately 2 to 3%).
  • the invention relates to a method for treating chlorophyll plants. This process is characterized in that foliated parts of plants are brought into contact with an aqueous solution of magnesium acid carbonate, with a view to stimulating and / or renovating the photosynthetic activity of said plants.
  • plants are treated by spraying with an aqueous solution of magnesium acid carbonate. Care must be taken that the aqueous solution of magnesium acid carbonate is sufficiently diluted, that is to say that it contains less than 80 g / l, preferably about 20 g / l of magnesium acid carbonate. .
  • the process for treating plants is even more effective when the composition also contains at least one trace element chosen from manganese, copper, zinc, boron, molybdenum and iron.
  • This or these trace elements are generally added in the form of carbonates, sulfates, nitrates or chloro- rures.
  • copper sulphate or ferrous iron chloride is added.
  • the treatment according to the invention accelerates the photosynthetic process of all plants, both wild and herbaceous. It activates the photosynthesis of chlorophyll plants and combats their magnesium deficiencies.
  • Surfactants are advantageously added to the solution to improve the penetration of one or more compounds by the leaves or needles of said plants.
  • the use of the above composition as activator and / or restorer of photosynthetic activity is effected by contact on the leaves.
  • the composition contains less than 80 g / l, preferably 20 g / l, approximately 20 g / l of magnesium acid carbonate.
  • the above composition can also be used for the treatment of plants suffering from magnesium deficiency or as a complementary magnesium fertilizer.
  • the invention also relates to a process for preparing a composition for the treatment of plants, containing an aqueous solution of magnesium acid carbonate of formula Mg (HC0,) .-, according to which one suspends in water in a reactor, of pure artificial magnesium oxide, of high reactivity, prepared by calcination of hydromagnesite at approximately 600 C C or by calcination of magnesium hydroxide at approximately 450 C C, as described in a work by Paul PASCAL, "New Treaty of Mineral Chemistry" Volume IV, 1958, Ed.
  • the refroid ⁇ says and maintains the temperature of the water and the solution at a temperature between 0 and 10 "C under a pressure of 5 to 6 bars in order to reach a concentration of 80 g / 1 of Mg (HC0 2 ) 2 , and ensure the stability of the solution until the moment of use.
  • the preparation of the concentrated solution of Mg (HC0 2 ) 2 is effected in a mobile unit close to the spraying zones of the diluted solution of Mg (HC0 2) 2.
  • an apparatus for the preparation of a composition for the treatment of plants according to the invention, comprising:
  • a main reactor provided with a means intended for the absorption of carbon dioxide and the transformation of magnesium oxide into magnesium acid carbonate, and conduits intended to bring the magnesium oxide into suspension of the tank to the main reactor and carbon dioxide from the tank to the main reactor.
  • This apparatus is distinguished from known apparatus by the fact that it is fixed on a mobile support in order to allow the extemporaneous preparation of the solution of
  • Mg (HC0,) _ at places close to the spray zones of the diluted solution of Mg (HC0,) _.
  • FIG. 1 shows the kinetics as a function of time of the photochemical component of chlorophyll fluorescence (qQ) in an unstressed leaf of durum wheat;
  • FIG. 2 shows the evolution of the photochemical component (qQ) of the extinction of chlorophyll fluorescence during the induction of light, on winter wheat, after application of Mg (HC0,) _;
  • FIG. 3 shows the evolution of the energy component (qE) of the extinction of chlorophyll fluorescence during the induction of light, on winter wheat, after application of Mg (HC0,) _;
  • FIG. 4 shows the spatial structure of the constituents of a photosynthetic device in mem ⁇ branes
  • - Figure 7 shows the evolution of the photochemical component of the extinction of the modulated chlorophyll fluorescence (relative gQ) over time
  • - Figure 8 illustrates the evolution of the photochemical component of the extinction of the fluorescence of chlorophyll during induction (qQ rel.), 0, 1, 4 and 150 days after spraying with a Mg solution (HC0 3 ) 2 on treated spruce compared to that of a control spruce letting appear symptoms of decay;
  • FIG. 10 shows the evolution of the sugar yield (kg / ha) of the sugar beets treated with the aid of Mg (HC0-j) 2 as a function of the application of increasing doses of Mg (HC0_ ) _;
  • FIG. 11 schematically shows a mobile unit for the extemporaneous production of magentaium carbonate.
  • Magnesium acid carbonate is an intermediate product, soluble in water, formed during the production of basic magnesium carbonate according to the PATTINSON process, (see GB-A-9102) or a similar process derived from it (see W0 -A-84 03 490).
  • the PATTINSON process uses as starting material dolomite or magnesite contaminated with calcium oxide.
  • dolomite or magnesite contaminated with calcium oxide.
  • the magnesium in the form of magnesium acid carbonate which is subjected to pressure filtration in order to retain the insoluble calcium carbonate. After filtration, the magnesium acid carbonate solution under CO 2 pressure is expanded.
  • the process described in document WO-A-84 03 490 uses as the starting material magnesite contaminated with iron.
  • the starting magnesite is treated by carbonation in an aqueous solution with a view to converting the magnesium to magnesium carbonate soluble in water under CO 2 pressure and the iron to insoluble ferrous carbonate.
  • the insoluble compound is removed by filtration under CO 2 pressure. After filtration, the magnesium carbonate solution, freed from iron, is relaxed.
  • the solution of magnesium acid carbonate was first diluted, before expanding it to atmospheric pressure, in order to ensure the chemical stability of the magnesium acid carbonate and to avoid its transformation into basic carbonate.
  • the photochemical component of the chlorophyll fluorescence is determined using a PAM 101-102-103 fluorimeter constructed by the company Waltz (Effeltrich, RFA) using modulated fluorescence and induced fluorescence.
  • An example of a fluorescence curve measured using this fluorometer is shown in fig. 1.
  • the modulated fluorescence is obtained by short pulses of red light (lys) applied at a frequency of 1.6 kHz.
  • An excitation light (A) of very low in-
  • This excitation light (A) makes it possible to measure the initial level of the fluorescence Fo.
  • the induction of chlorophyll fluorescence is caused by a second light, white (B), unmodulated and further
  • the quantum yield (rQ) is a measure of the efficiency of the transformation of light energy into chemical energy by photosynthesis. It measures the number of moles of 0 produced (or C0 fixed) per mole quanta of photosynthetically active radiation.
  • Table 1 Results of the quantum yield (rQ) measurements on plants not deficient in magnesium (controls) and plants deficient. Standard deviations are mentioned in parentheses.
  • Table 1 shows a significant decrease (about 55% of the control) in the production of * * in plants deficient in magnesium, which indicates a significant inhibition of photosynthetic activity probably due to an alteration in photo ⁇ chemical processes. chloroplasts due to magnesium deficiency.
  • Figure 2 shows the evolution of the photochemical component (qQ) of the extinction of chlorophyll fluorescence during the induction of light, over time on winter wheat, after application of Mg (HC0,) _ on control plants F, having received a nutrient solution containing magnesium, on deficient plants G having received a nutrient solution free of magnesium and on treated plants J having received a nutrient solution free of magnesium but having been treated by foliar spraying with an aqueous solution containing 20 g / 1 of acid carbonate magnesium.
  • Figure 3 shows the evolution of the energy component (qE) of the extinction of chlorophyll fluorescence during induction after six days of treatment on winter wheat.
  • Table 2 Results of the photochemical extinction measurements of the fluorescence of chlorophyll (qQ) on plants not deficient in magnesium (controls) and plants deficient. Standard deviations are mentioned in parentheses.
  • Table 2 indicates a strong inhibition of the reoxidation of the primary acceptors of the PS2 photoreceptor system. These results reveal important changes in the ultra-structure of the chloroplasts.
  • CHEVALIER and HUGUET (1975) studying the effects of magnesium deficiency on the ultra-structure of chloroplasts in apple leaves have found that an inadequate magnesium diet leads to a deformation of the lamellar structure of the chloroplasts.
  • magnesium is a stabilizing element of the thylacoid membranes of chlo ⁇ roplasts.
  • this lamellar structure is very important in the structural organization of the electron transfer chain.
  • FIG. 4 shows the spatial organization of the constituents of the photosynthetic apparatus in the thylacoid membranes composed of three types of chloroprotein complexes as represented in a publication by ANDERSON and ANDERSON in 1982.
  • the photoreceptor system PS 1 which is a photosystem characterized by the trap pigment P 700;
  • the PS 2 photoreceptor system which is a photosystem characterized by the trap pigment P 680.
  • the junction between PS 2 and PS 1 is carried out by a chain of electron transporters composed of quinones (Q), plastoquinones (PQ), cytochromes (Cyt) and plastocyanines (PC).
  • Q quinones
  • PQ plastoquinones
  • Cyt cytochromes
  • PC plastocyanines
  • FIG. 4 shows that the PS2 photoreceptor systems are confined in stacked areas 1 while all of the PSI photoreceptor systems are located in non-stacked areas 2 of the thylacoid membranes; the disorganization of this arrangement therefore results in an inhibition of the transfer of electrons in the chain and therefore an inhibition of the photosynthetic activity of the plant.
  • THOMSON and WEIR (1962) have found in Phaseolus vulgaris magnesium deficiency, a decrease in the number of grana and a reduction or total absence of their compartmentation. They also found an accumulation of starch grains.
  • the corn and the barley were cultivated in cylindrical pots of 25 cm in diameter and 70 cm in height on inert substrate (quartz) and fed with a nutritive solution without magnesium to induce the deficiency and whose composition is as follows:
  • the first row normally supplied with magné ⁇ sium serves as a control.
  • Quantum yield (rQ) and chlorophyll fluorescence (qQ) measurements were taken on four rows of magnesium-deficient corn plants, the first (F) untreated, the second (G) treated with foliar spray with a solution containing 20 g / l of magnesium acid carbonate, the third sprayed with a solution of magnesium chloride and the fourth sprayed with a solution of sodium bicarbonate. The results are those measured 0, 4 and 10-15 days after foliar spraying.
  • Figure 5 illustrates the increase in quantum yield in
  • Measurements of the photochemical component (qQ) were made 0, 1, 4, 6 and 10-15 days after spraying on untreated control plants (K) and on the four rows of magnesium-deficient corn plants, the first (L) untreated, second (M) treated by foliar spraying with an aqueous solution containing 20 g / 1 of magnesium acid carbonate, the third (N) sprayed with a solution of magnesium chloride and the fourth (0) sprayed with an aqueous solution of 20 g / 1 of sodium bicarbonate (Figure 6).
  • the technique consists of enclosing a leaf disc in a room where the circulating air flow is controlled.
  • the carbon monoxide C0 2 from the air can be removed using a sodium hydroxide column (NaOH) and the photosynthetic activity is followed by measuring the chlorophyll fluorescence (qQ).
  • qQ chlorophyll fluorescence
  • the leaf discs were cut from barley leaves (at the 2-leaf stage).
  • the evolution of the photochemical component of the extinction of the chlorophyll fluorescence over time immediately after the induction of light is illustrated in FIG. 7.
  • the control curve, (denoted P) corresponds to a test during which the air circulating in the room is not rid of its CO_.
  • the curve relating to the treated barley (denoted T) corresponds to a test during which the air is relieved of its CO-, thanks to the absorption of the latter on a column of soda.
  • FIG. 7 shows that in the absence of CO 2 in the air, the disturbance of the chlorophyll fluorescence qQ over time for the treated discs (curve S) is much lower than for the control discs (curve T).
  • the restoration of qQ for the treated discs (curve S) can only be explained by an intra-leaf release of C0 2 by Mg (HC0,) 2 .
  • This intra-foliar release of C0 2 in the leaves would act as a boost for plants deficient and treated with Mg (HC0 3 ) 2 , which allows an acceleration of the recovery of activity. quickly photosynthetic found in previous tests.
  • the results are represented in the form of a graph in FIG. 8.
  • the control test represented by line V reveals a relatively constant modulated fluorescence, while the test relating to samples of young spruces affected by "acid rain" and treated with a solution of magnesium acid carbonate is represented by line U.
  • Line E shows a restoration of photosynthetic activity seven days after treatment with said solution.
  • the needles of the treated trees regain a dark green color after only four days. This indicates that in the case of fir needles the penetration of magnesium in the "Mg (HC0 3 ) 2 " form is very rapid.
  • After four months of treatment the production of young shoots was noted and in the fifth month these shoots have reached a length of 10 to 15 cm. This indicates a spectacular and effective recovery of these young fir trees when the control trees did not form shoots or formed extremely short shoots which hardly exceeded 1 cm in length and which quickly took on a yellow color. .
  • the tests are repeated four times.
  • the test n c 1 relates to control plants in the absence of any foliar spray of a composition of magnesium acid carbonate.
  • Test No. 2 relates to plants treated by foliar spraying with an acid composition of magesium at a rate of 3 kg Mg / ha (ie 5 liters of an aqueous solution containing 25 g / 1 of Mg (HCO,) 2 or 7.15 g / 1 of magnesium per elementary plot of 120 m).
  • the treatment was carried out at the last leaf stage so as to prolong and stimulate the photo-synthetic activity and ensure better filling of the grain in the absence of scalding phenomena.
  • Test No. 1 relates to control plants without foliar spraying of a composition of magnesium acid carbonate.
  • Test No 2 relates to seed potatoes treated by spraying
  • the increase in dry matter yield is 13.8% compared to the untreated control.
  • Test No. 1 relates to corn control plants, in the absence of any foliar spraying of a composition of magnesium acid carbonate.
  • Test No. 2 relates to corn plants treated by foliar spraying with a composition of magnesium acid carbonate at a rate of 3.5 kg Mg / ha (ie 6 liters of an aqueous solution containing 25 g / 1 Mg (HCO,) _ or 7.15 g / 1 Mg per elementary plot of 120 m).
  • the plot is contiguous to the plot planted with potatoes, which is the subject of the tests mentioned under 2) above.
  • the levels of exchangeable nutrients and the pH are in order and no magnesium deficiency of pedological origin has been demonstrated.
  • Test No. 1 relates to control plants in the absence of any spraying of a composition of magnesium acid carbonate.
  • Tests No. 2, 3 and 4 relate to sugar beet plants subjected respectively to one, two and three foliar sprays of a composition of magnesium acid carbonate.
  • the magnesium dose is theoretical.
  • the product is applied in the pure state without taking into account the percentage of precipitation. Application is made at the 10-12 leaf stage before coverage.
  • FIG. 9 illustrates the evolution of the root yield as a function of the dose of magnesium applied in the form of Mg (HCO -.) .-.
  • Figure 10 shows that the sugar yield per hectare increases with the application of increasing doses of product. This sugar yield / ha increases even better than for the root yield: 26.6% at the application rate of 10.5 kg Mg (HC0 3 ) 2 / ha (theoretical dose of 3 Kg Mg / ha) .
  • Mg (HC0_) 2 is a product which, optimally developed and well "targeted "phytotechnically, offers significant prospects for agricultural development.
  • the present invention also relates to a process for preparing a composition for the treatment of plants containing an aqueous solution of magnesium acid carbonate Mg (HC0 _) _.
  • pure magnesium oxide of high reactivity with respect to gaseous carbon dioxide is mixed in a reactor with water, so as to obtain a suspension and the suspension thus obtained is treated with l carbon dioxide gas under pressure, at a temperature below 40 ° C, preferably at a temperature of about 10 ° C and under partial pressure in carbon dioxide
  • This step of the process is similar to a process described in document O-A-8 403 490 relating to the preparation of magnesium carbonate trihydrate and basic magnesium carbonate.
  • the slightly reactive magnesite obtained by calcination at high temperature, that is to say beyond 800 ° C.
  • artificial pure magnesium oxide obtained in the form of a finely divided powder with high reactivity towards C0_ and a specific surface
  • the magnesium oxide is mixed with water and the suspension thus obtained is treated with CO 2 gas injected into the top of a reactor.
  • the reactor is maintained at a pressure in
  • the reaction product is diluted with water, in order to avoid any untimely precipitation of the basic magnesium carbonate, so as to obtain a dilute solution containing less than 80 g / l of magnesium carbonate, preferably about 20 g / l of magnesium carbonate.
  • the second stage of the process consists in expanding the dilute aqueous Mg (HCO _) _ solution to atmospheric pressure.
  • the result of this dilution is to present the composition in an appropriate form and concentration allowing its immediate use as an activator of the photosynthetic activity of plants by simple spraying on them.
  • This process according to the invention uses magnesium oxide with a particle size of less than 20 microns, preferably grains of about 10 microns.
  • FIG. 11 Apparatus suitable for the preparation of a solution of magnesium acid carbonate according to the invention in a batch manner by successive charges is shown diagrammatically in FIG. 11.
  • This apparatus comprises a tank R fi intended for dispersing finely ground magnesium oxide in suspension in water, a reservoir R. of carbon dioxide
  • Each of the reactors R 2 , R-. includes detectors of the filling level N .., N 2 ' N ⁇ N and ° ⁇ es measuring devices P., P-. of the pressure prevailing in them.
  • Magnesium oxide is suspended in water and the reactor R2 is filled to the NI level. As soon as the NI level is reached, the level detector controls the closing of the valve Vo, the opening of the valve VI (by commissioning the transmitter Pi) and the starting of the agitator. The other valves V effetto V, are kept closed.
  • the reactor R2 begins to transfer.
  • the residual CO- suspension in the main reactor R- makes it possible to discharge the aqueous magnesium carbonate solution to the transfer reactor R_ ,.
  • the main reactor R_ is connected, 0 to a transfer reactor R_. by a conduit 5 located near its lower part and the transfer reactor R 3 is a closed enclosure provided at its upper part with a conduit 4 for supplying gaseous carbon dioxide so as to put, r, this enclosure under pressure from above.
  • the enclosure is advantageously provided with a vent V. and means V_, P_ and N_ intended for regulating the pressure prevailing in the enclosure and the level of liquid in the enclosure.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Fertilizers (AREA)
  • Compounds Of Unknown Constitution (AREA)
  • Steroid Compounds (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
EP90906787A 1989-05-31 1990-05-30 Zusammensetzung zur behandlung von pflanzen und deren anwendung Expired - Lifetime EP0474649B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
BE8900589 1989-05-31
BE8900589A BE1003937A3 (fr) 1989-05-31 1989-05-31 Composition de carbonate acide de magnesium et utilisation.
PCT/BE1990/000024 WO1990015037A1 (fr) 1989-05-31 1990-05-30 Composition pour le traitement de vegetaux et utilisation de celle-ci

Publications (2)

Publication Number Publication Date
EP0474649A1 true EP0474649A1 (de) 1992-03-18
EP0474649B1 EP0474649B1 (de) 1994-06-29

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US (1) US5552366A (de)
EP (1) EP0474649B1 (de)
AT (1) ATE107917T1 (de)
AU (1) AU5658390A (de)
BE (1) BE1003937A3 (de)
CA (1) CA2057030A1 (de)
DD (1) DD294845A5 (de)
DE (1) DE69010334T2 (de)
DK (1) DK0474649T3 (de)
ES (1) ES2057560T3 (de)
FI (1) FI102164B1 (de)
HU (1) HU216798B (de)
IE (1) IE65327B1 (de)
NO (1) NO301069B1 (de)
PL (1) PL164820B1 (de)
PT (1) PT94230A (de)
WO (1) WO1990015037A1 (de)

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CN104886128A (zh) * 2015-05-14 2015-09-09 昆明理工大学 镁离子在提高植物光合效率中的应用

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AT392267B (de) * 1989-01-13 1991-02-25 Radex Heraklith Verfahren zur herstellung eines mittels zur bodenmelioration aus mgo und mbco3
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WO2004040981A1 (en) * 2002-10-23 2004-05-21 Radical Waters (Ip) (Pty) Limited Method for enriching co2 concentrations in a plant environment

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CN104886128A (zh) * 2015-05-14 2015-09-09 昆明理工大学 镁离子在提高植物光合效率中的应用

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ES2057560T3 (es) 1994-10-16
PT94230A (pt) 1991-02-08
PL285414A1 (en) 1991-01-14
PL164820B1 (pl) 1994-10-31
BE1003937A3 (fr) 1992-07-22
US5552366A (en) 1996-09-03
HUT61957A (en) 1993-03-29
FI102164B (fi) 1998-10-30
AU5658390A (en) 1991-01-07
DE69010334D1 (de) 1994-08-04
IE901943L (en) 1990-11-30
DE69010334T2 (de) 1995-02-16
HU216798B (hu) 1999-08-30
NO914723D0 (no) 1991-11-29
FI915612A0 (fi) 1991-11-28
IE65327B1 (en) 1995-10-18
WO1990015037A1 (fr) 1990-12-13
DK0474649T3 (da) 1994-08-15
ATE107917T1 (de) 1994-07-15
CA2057030A1 (en) 1990-12-01
FI102164B1 (fi) 1998-10-30
NO914723L (no) 1992-01-17
DD294845A5 (de) 1991-10-17
NO301069B1 (no) 1997-09-08
HU904254D0 (en) 1992-04-28
EP0474649B1 (de) 1994-06-29

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